rs1003199
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs1003199(C;C) |
Make rs1003199(C;T) |
Make rs1003199(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 159328558 |
Gene | IL12B |
is a | snp |
is | mentioned by |
dbSNP | rs1003199 |
dbSNP (classic) | rs1003199 |
ClinGen | rs1003199 |
ebi | rs1003199 |
HLI | rs1003199 |
Exac | rs1003199 |
Gnomad | rs1003199 |
Varsome | rs1003199 |
LitVar | rs1003199 |
Map | rs1003199 |
PheGenI | rs1003199 |
Biobank | rs1003199 |
1000 genomes | rs1003199 |
hgdp | rs1003199 |
ensembl | rs1003199 |
geneview | rs1003199 |
scholar | rs1003199 |
rs1003199 | |
pharmgkb | rs1003199 |
gwascentral | rs1003199 |
openSNP | rs1003199 |
23andMe | rs1003199 |
SNPshot | rs1003199 |
SNPdbe | rs1003199 |
MSV3d | rs1003199 |
GWAS Ctlg | rs1003199 |
GMAF | 0.3669 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 23164360] Association of IL12B polymorphisms with susceptibility to Graves ophthalmopathy in a Taiwan Chinese population